- REGULATORY *** CONTRACT *** Brussels >> Regulatory Consultant with good RA project management skills
If you wish to apply for this role, please send your CV with a covering note to email@example.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
- Senior RA Officer
I am working with a pharmaceutical company based on the outskirts of London who is searching for a Senior RA Officer to join their team on an initial 4 month contract to start ASAP. There are a couple of key points that must be met, they are as follows -- European regulatory submissions experience.- Experience dealing directly with the EMA.- MRP & DCP experience.
- Ophthalmology Hospital Specialist - N London / Berks / Surrey
This award winning and highly acclaimed Blue Chip Pharmaceutical Company are at the cutting edge of patient care. They have one of the strongest product pipelines within the industry, currently with 70 products at phase three and beyond and are much admired and respected and are set to become the largest supplier of prescription medicine by 2017.An opportunity has become available for a Hospital Specialist to promote within their Glaucoma and Dry eye division.
- FR SPEAKING CMC RA BIO *** Permanent role ** Switch from CMC lifecycle subs to CMC RA Bio Dev >> Sr Manager Role
I am working with a really profound manager who has very strong in terms of their knowledge of the global requirements and EU specific pathway, ie, how regulatory CMC supports CMC packages in development through scale up, registration and for new lifecycle ...
- Launch Excellence Project Manager
Launch Excellence Project Manager An exciting opportunity has become available within a leading global healthcare company that is dedicated to, and fundamentally passionate about, changing...
- OPTION BELGQIUE *** RA Contractor EU Lifecycle Part time 50%
We have a late breaking contractor role for Brussels, 20 hours per week, good rate, start immediately!
The role is working on Centralised Procedure products, and this is a requirement.
- Regulatory Affairs / Regulatory / RA / Project Management / Manager / ISO 13485 / Medical Devices /
Job Title: Regulatory Affairs Project ManagerLocation: WiltshireSalary: £50,000 - £65,000This position is responsible for managing all facets of regulatory support to market products, developing regulatory submissions, managing departmental projects. In addition, the position will supervise the development and creation of labelling, provide guidance and consultation for domestic and international regulations and interact with governmental agencies. ...
- OPTION BENELUX *** Regulatory ONCOLOGY Associate Director *** P2B / P3 NMEs, mAbs, ADCs, Nibs >> Sr RA Project Manager MULTIPLE filings!
OPTION BENELUX *** Regulatory ONCOLOGY Associate Director *** P2B and P3 NMEs, mAbs, ADCs, Nibs >> Senior RA Project Manager MULTIPLE filing Opportunities
- Senior Project Manager/ Launch Facilitator, Global Projects
The Launch Facilitator will coordinate and lead the Launch of Late Phase Full Service Studies (i.e., those awards including Project Management and at least one other service). The Launch Facilitator supports the Global Project Lead (GPL) and Project Team and is accountable for the quality, timeliness, and effectiveness of the Launch process. The Launch process starts immediately after the BD handoff meeting and ends with delivery of the final outputs of the Launch meeting.
- Senior Project Manager/Launch Facilitator for Global Projects
Due to continued growth Worldwide Clinical Trials (WCT) have a vacancy for a Launch Facilitator, Global Projects.
Permanant, Nottingham office based.
The Launch Facilitator will coordinate and lead the Launch of Late Phase Full Service Studies (i.e., those awards including Project Management and at least one other service).